IRCT20180620040164N58尚未招募Unknown
Randomized, single-dose, crossover comparative bioequivalence study of Omeprazole 20 mg tablet of ACTOVERCO and Hexal in 24 healthy male under fasting conditions
ACtover Pharmaceutical Co.0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 24
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 years 至 45 years(—)
- 性别
- Male
入选标准
- •Healthy subjects (male) should be between 20-45 years old.
- •subjects how have body mass index (BMI) Within 15% of normal range between 18.5-30 (Kg/m2)
- •Subjects with normal vital signs.
- •Subjects who agree with patient consent form.
排除标准
- •Subjects with known allergy to the products tested.
- •Subjects must not have a historical specific diseases or abnormal values in labratory tests and general clinical examination.
- •Chronic or acute diseases of the digestive system, such as diseases related to the esophagus, gastritis, peptic ulcer, intestinal inflammation, bleeding in the digestive tract, or digestive system surgery during the last three years.
- •Having problems with vascular system, endocrine system, nervous system, digestive system, respiratory system, blood system, immune system, mental and metabolic system.
- •Performing surgery within 4 weeks before drug administration or at the time of clinical study.
- •Smoking more than 10 cigarettes per day, losing more than 500 ml of blood in less than 7 days.
- •A history of difficulty with donating blood or donation of more than 500 ml blood within 7 days prior to the start of the study.
研究者
相似试验
已完成
不适用
bioequivalence study of Metformin 100 mg + Sitagliptin 50 mg tablets in 24 healthy male under fasting conditionsIRCT20180620040164N15Actover co24
已完成
不适用
Bioequivalence study of Ondansetron 4 mg film-coated tablet in 24 healthy male under fasting conditionsIRCT20180620040164N2Aburaihan pharmaceutical co.24
招募中
不适用
Study of absorption and elimination rate of Gefitinib 250 mg tablets in comparison with standard tablet of Iressa® (AstraZeneca company).IRCT20200407046981N6Kimia pharmaceutical Co30
已完成
不适用
Bioequivalence study of Linagliptin 5 mg tablets in 24 healthy male under fasting conditionsIRCT20180620040164N4Alhavi pharmaceutical co.24
招募中
不适用
Study of absorption and elimination rate of Imatinib 400 mg capsules in comparison with standard tablet of Imatinib (Gleveec).In this study, the disease is not examined. The subject of the study is the bioequivalence study of the Imatinib capsules of test and reference in healthy volunteers..IRCT20200407046981N9Kimia pharmaceutical Co30
